ABG-HM-1 Hummi Micro Draw Blood Transfer Device Product Usage: It is… — Class I medical device recall Z-1636-2016
Terminated recall by Hummingbird Med, reported 2016-06-01, distributed in CA, GA, IL, KY, MD. Hummingbird Med Devices, Inc. is recalling ABG-HM-1 Hummi Micro Draw Blood Transfer because the connection bet
| Recall number | Z-1636-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hummingbird Med, Lake Forest, CA, United States |
| Recall initiated | 2015-10-01 |
| Classified | 2016-05-20 |
| Reported by FDA | 2016-06-01 |
| Terminated | 2017-01-26 |
| Distributed | CA, GA, IL, KY, MD |
| Quantity | 11,500 units |
| Lot numbers | 15180, 15286, 15287, 15300, 15305 |
Product
ABG-HM-1 Hummi Micro Draw Blood Transfer Device Product Usage: It is used for blood transfer and collection from Peripheral Arterial Line Catheters.
Reason for recall
Hummingbird Med Devices, Inc. is recalling ABG-HM-1 Hummi Micro Draw Blood Transfer because the connection between the "Hummi" Y connector and the yellow cannula hub may not be sufficiently secure enough and could separate while in use.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1636-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.